Immunome, Inc. logo

Executive Director, Clinical Development

Immunome, Inc.
Full-time
Remote friendly (Bothell, WA)
United States
$385,000 - $425,000 USD yearly
Clinical Research and Development

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Role Summary

Executive Director, Clinical Development. The role provides strategic direction and oversight for the clinical development of Immunomeβ€šΓ„Γ΄s oncology pipeline, from early development through late-stage trials, and represents the company with regulators and external stakeholders.

Responsibilities

  • Provide strategic clinical leadership and responsibility for all clinical deliverables.
  • Develop protocols aligned with Clinical Development Plans (CDP), regulatory documents, and medical communications.
  • Manage operational aspects and drive execution of the clinical program in partnership with other functions.
  • Manage budget and resources with the CMO and Project Managers to ensure timely deliverables.
  • Engage with external stakeholders (regulatory authorities, key opinion leaders, advisory boards, patient groups) and internal decision boards.
  • Develop and maintain relationships with internal and external scientific experts to represent the company clinically.
  • Support the CMO in ensuring overall safety of the compound in collaboration with the Safety Leader.
  • Stay current with clinical and drug development information through literature review and scientific meetings.
  • Lead development and implementation across program-specific standards.

Qualifications

  • M.D. with clinical research experience in oncology required.
  • Minimum 10+ years of clinical development experience in oncology.
  • Proven track record of advancing oncology programs through pivotal/registrational trials; prior leadership in large pharma or biotech strongly preferred.

Knowledge And Skills

  • Deep expertise in oncology clinical trial design and execution across early and late-stage studies.
  • Thorough knowledge of FDA, EMA, and ICH regulations for oncology drug development; proven ability to lead regulatory interactions globally.
  • Ability to design, run, and analyze global clinical studies.
  • Strong understanding of translational medicine, clinical pharmacology, and integration of biomarker insights into development strategy.

Education

  • Not specified in the description.
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